Phase 2 study of weekly bortezomib in mantle cell and follicular lymphoma Journal Article


Authors: Gerecitano, J.; Portlock, C.; Moskowitz, C.; Hamlin, P.; Straus, D.; Zelenetz, A. D.; Zhang, Z.; Dumitrescu, O.; Sarasohn, D.; Lin, D.; Pappanicholaou, J.; Cortelli, B. M.; Neylon, E.; Hamelers, R.; Wright, J.; O'Connor, O. A.
Article Title: Phase 2 study of weekly bortezomib in mantle cell and follicular lymphoma
Abstract: Twice-weekly bortezomib has proven activity in mantle cell (MCL) and indolent lymphomas. This study explored a weekly schedule of bortezomib in follicular lymphoma (FL) and MCL. Although weekly bortezomib was better tolerated, the overall response rate (ORR) was inferior (18% vs. 50%, P = 0.02) with no complete remissions (CR) (compared with 18% CR for the twice-weekly schedule). Progression-free survival (PFS) was not different. The weekly schedule of bortezomib was less toxic, but yielded fewer and lower quality responses than twice-weekly bortezomib. Given the similar PFS, the weekly schedule may still be appropriate for some patients.
Keywords: aged; aged, 80 and over; disease-free survival; middle aged; clinical trial; antineoplastic agents; disease free survival; antineoplastic agent; bortezomib; phase 2 clinical trial; boronic acids; protease inhibitors; pyrazines; follicular lymphoma; boronic acid derivative; proteinase inhibitor; pyrazine derivative; lymphoma, follicular
Journal Title: British Journal of Haematology
Volume: 146
Issue: 6
ISSN: 0007-1048
Publisher: John Wiley & Sons  
Date Published: 2009-09-01
Start Page: 652
End Page: 655
Language: English
PUBMED: 19624539
PROVIDER: scopus
PMCID: PMC4035037
DOI: 10.1111/j.1365-2141.2009.07775.x
DOI/URL:
Notes: --- - "Cited By (since 1996): 3" - "Export Date: 30 November 2010" - "Source: Scopus"
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MSK Authors
  1. Zhigang Zhang
    428 Zhang
  2. Carol Portlock
    204 Portlock
  3. Craig Moskowitz
    407 Moskowitz
  4. Andrew D Zelenetz
    767 Zelenetz
  5. Paul Hamlin
    277 Hamlin
  6. David J Straus
    356 Straus
  7. Dorothy S Lin
    4 Lin